Sineth is a 13-year-old 8th grade student from Kampong Cham Province in Cambodia. She lives with her parents and younger sister, who is in Grade 4. Her parents are rice farmers and work hard to support their family. Sineth enjoys studying Khmer literature, which is her favorite subject at school, and hopes to become a doctor in the future. In her free time, she likes listening to music and chatting with her friends. Her favorite food is fried pork with ginger. Sineth has scoliosis, a condition in which the spine curves abnormally to one side, often resembling a "C" or "S" shape. Her spinal curve has gradually worsened over the past three years and is now approximately 50 degrees in the thoracolumbar region. Although she does not currently experience pain, the increasing curvature affects her posture and makes it difficult for her to sit comfortably for long periods. This can make it harder for her to stay comfortable and concentrate during class, and the curvature may continue to worsen as she grows. Sineth's family was referred to our medical partner, Children’s Surgical Centre (CSC), by another hospital. They traveled approximately four hours from Kampong Cham to seek specialized care. On August 17th, surgeons at CSC plan to perform posterior spinal fusion to help straighten and stabilize her spine and prevent the curvature from worsening. She needs $1,500 in support to cover the cost of her surgery and related medical care. This treatment will help support her spinal health as she continues to grow and allow her to remain active and continue her education. Sineth's parents said, “We hope that this surgery will help straighten and stabilize our daughter’s spine and prevent her scoliosis from getting worse. We wish for her to grow well, stay active, and continue her studies and daily activities with confidence and comfort.”

Akai is a four-year-old girl from Kenya. She is the third-born in a family of four children. Akai experiences misalignment of her legs, and due to financial challenges, she has not been able to receive treatment for her condition before. Akai's condition was not noticeable until she began walking. Her mother noticed her legs were bowed, which made it difficult for her to run and play comfortably, and has led to isolation from her peers. Her guardian shared that Akai is supposed to start school soon, but due to the stigmatization she has been facing, it might be difficult for her to do so until she receives treatment. Fortunately, Akai was able to connect with our medical partner's hospital for review and treatment. On May 21st, she will undergo surgery to correct her condition and improve her quality of life. Our medical partner, African Mission Healthcare, is requesting $1,224 to cover the cost of Akai's procedure and care. Akai's guardian said, "We will be grateful to see her walking like other children."

Hikma is a charming 20-month-old girl who lives with her parents and older brother in Ethiopia. Her parents were small-scale farmers until they were displaced due to war in their area. Now, her mother is a dedicated home maker, and her father works as a daily laborer. As with many other displaced families, it has been difficult for them to afford their daily necessities. Hikma was born with an anorectal malformation, a congenital condition that can lead to a complete or partial intestinal blockage. However, the symptoms were not obvious until she was around one year old. Her mother was deeply distressed by what she observed and immediately informed Hikma’s grandmother, who then began seeking for medical assistance. To avoid social stigma, however, the family tried to keep Hikma’s condition private. Eventually, the grandmother came across a Catholic missionary organization, which connected the family with a field coordinator of our medical partner's care center, BethanyKids Myungsung Christian Medical Centre (BKMCM). With the support of relatives and the Catholic missionaries, Hikma's family raised funds to travel to Addis Ababa. Upon arrival at the hospital, doctors explained that Hikma would need a series of surgeries to eliminate bowel dysfunction. The family was relieved and encouraged to hear that Hikma could be helped. Presently, Hikma has already undergone the first surgery, a colostomy creation, and recovered well. Now, Hikma needs support for her second surgery, which will occur on April 20th. Our medical partner, African Mission Healthcare Foundation, is requesting $1,500 to cover the total cost of Hikma's procedure and care. After her recovery, Hikma will no longer experience bowel dysfunction or be at risk of developing health complications in the future. Hikma’s mother said, “I would like to thank you sincerely for your support and the services you provided. Thank you again. I truly hope my child will grow up to be a wonderful woman.”

Mitchelle is a 12-year-old girl from Kenya. She is shy but determined. Mitchelle is in eighth grade and dreams of becoming a teacher one day. Her inspiration comes from her English teacher, whose passion and eagerness in the classroom motivate Mitchelle to pursue the same path and help others learn. We met Mitchelle at CURE Children’s Hospital, where she had come for treatment, accompanied by her parents. Her mother is a peasant farmer who works hard to support the family and ensure her children have the opportunity to go to school. Mitchelle was born healthy and grew up like any other child. However, last year, while visiting her aunt, something unusual was noticed. As Mitchelle bathed, her aunt noticed a pronounced bend in her spine, affecting her posture while standing, walking, and causing pain while bending. Concerned, she immediately informed Mitchelle’s parents and advised them to seek medical help. Her aunt also told them about the CURE mobile clinic in Kabarnet, encouraging them to attend so that Mitchelle could be examined by specialists. Physicians at AIC Cure International Hospital determined that Mitchelle should undergo a procedure called a spinal fusion. This surgery fuses two or more unstable vertebrae together to reinforce the back structure with the goal of reducing pain and easing symptoms. Our medical partner, African Mission Healthcare, is requesting $1,500 to fund this procedure. The treatment is scheduled to take place on March 19th, and once completed, it will hopefully improve Mitchelle's quality of life. “I am looking forward to getting better so that I can stand upright, return to school comfortably, and continue working hard to become a teacher one day,” Mitchelle shared softly.

Swalehe is a two-year-old boy from Tanzania. He lives with his parents and two older siblings. His father earns a living pushing a market cart and transporting goods for customers, while his mother stays at home caring for the children and managing the household. Swalehe was born with fused fingers on both hands and fused toes on his left foot. As he has grown, these conditions have affected the development of his fine motor skills and his balance when walking and playing. Initially, the family was not sure if these conditions could be treated. Thankfully, they learned about our medical partner's care center, Kafika House, through a friend whose child had received successful care there. The family travelled to Kafika House, where doctors recommended surgical treatment. Without treatment, Swalehe will continue to experience functional limitations. Fortunately, our medical partner, African Mission Healthcare, is helping Swalehe receive treatment. On February 18th, surgeons will perform contracture release surgery and a skin graft to give Swalehe the chance to grow, play, and develop with greater independence and confidence. Now, he needs help to fund this $832 procedure. Swalehe's mother says, “His fingers are joined and tight, so he cannot grasp or release objects properly.”

Loudmia is a preschooler from Haiti. She lives in a small coastal village in northwest Haiti with her four siblings and her parents, who both fish and farm. She enjoys going to preschool and playing with the children in her neighborhood. Loudmia has a cardiac condition called a ventricular septal defect. A hole exists between the two lower chambers of her heart; blood leaks through this hole without passing through her lungs to obtain oxygen, leaving her weak and short of breath. Loudmia will fly to the Dominican Republic to receive treatment. On January 21st, she will undergo cardiac surgery, during which surgeons will sew a patch over the hole so that blood no longer leaks through it. Our medical partner, International Cardiac Alliance, is contributing to pay for surgery. However, Loudmia's family also needs help to fund the costs of surgery prep. They need help raising $1,500 to cover labs, medicines, and check-up and follow-up appointments. This also supports securing travel documents for the family and travel costs for the social workers from our medical partner, who will accompany Loudmia's family overseas. Loudmia's mother shared, "I am hopeful that after this surgery we can stop worrying about our daughter's health so much!"

Eh Mu is a 26-year-old woman from Burma who lives with her husband, her parents, older sister, older brother, younger sister, younger brother, her son and her nephew in a refugee camp in Thailand. Eh Mu and her family fled to the refugee camp in 2022 due to an airstrike and fighting in her village. Her parents are retired while her older brother and husband sometimes went to work outside of the camp as day laborers, while her older sister looks after a dormitory in the camp. Her son is a nursery school student. Eh Mu is a homemaker and makes custom dresses on order. During her free time, Eh Mu loves to play with her three-year-old son, spend time with her family, and listen to music on her phone. Eh Mu is currently expecting her second child. Her doctors recommend that she deliver via a caesarean section because of a high-risk pregnancy. This way, doctors can ensure the safety of both mother and child. Our medical partner, Burma Children Medical Fund, is helping Eh Mu undergo a C-Section on December 22nd at our medical partner's care center, Tha Song Yang Hospital. This procedure will cost $1500, and Eh Mu needs your support. Eh Mu said, “When I noticed my pregnancy, I started feel stress instead of happy. I worry that if I need to deliver my baby through surgery, then I cannot afford to pay for the surgery. When I gave birth through c-section in Burma for my first baby, at that time the treatment cost is less but here in Thailand is very expensive for what I heard from my friend. At first, I was thinking of returning to Burma to give birth, but fighting continues in my village and it is not safe to return so I have no other option. After I learned from the doctor that there will be an organization who will support my surgery cost, I feel like all my stress and worries are gone. I am happy and thankful to BCMF and all their donors who are available for me during this difficult time”.

Yohane is a 12-year-old student from Tanzania. He comes from a large family of eight children, and his parents are small farmers who rely on the land for their livelihood. Despite his condition, Yohana has always shown a determined spirit and a bright smile. He had to drop out of school because of the challenges he faced walking to and from school. Yohane has clubfoot on his right foot, a condition in which the foot is twisted out of shape. The tissues connecting the muscle to the bones are shorter than usual and this causes difficulty walking and even wearing shoes. Fortunately, Yohane's family traveled to visit our medical partner's care center, Kafika House, where the medical team will begin clubfoot treatment on November 11th. Our medical partner, African Mission Healthcare, is requesting $1,119 to fund Yohane's clubfoot repair. After treatment, he will be able to walk easily. Yohane says, “I miss going to school with my friends.”